KU Leuven, Laboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine and Leuven Kanker Instituut, Campus Gasthuisberg O/N-1 B-802, Herestraat 49, B-3000 Leuven, Belgium.
KU Leuven, Laboratory of Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine and Leuven Kanker Instituut, Campus Gasthuisberg O/N-1 B-802, Herestraat 49, B-3000 Leuven, Belgium.
Biochim Biophys Acta Mol Cell Res. 2021 Jun;1868(7):119020. doi: 10.1016/j.bbamcr.2021.119020. Epub 2021 Mar 30.
Inside cells, the endoplasmic reticulum (ER) forms the largest Ca store. Ca is actively pumped by the SERCA pumps in the ER, where intraluminal Ca-binding proteins enable the accumulation of large amount of Ca. IP receptors and the ryanodine receptors mediate the release of Ca in a controlled way, thereby evoking complex spatio-temporal signals in the cell. The steady state Ca concentration in the ER of about 500 μM results from the balance between SERCA-mediated Ca uptake and the passive leakage of Ca. The passive Ca leak from the ER is often ignored, but can play an important physiological role, depending on the cellular context. Moreover, excessive Ca leakage significantly lowers the amount of Ca stored in the ER compared to normal conditions, thereby limiting the possibility to evoke Ca signals and/or causing ER stress, leading to pathological consequences. The so-called Ca-leak channels responsible for Ca leakage from the ER are however still not well understood, despite over 20 different proteins have been proposed to contribute to it. This review has the aim to critically evaluate the available evidence about the various channels potentially involved and to draw conclusions about their relative importance.
在细胞内,内质网 (ER) 形成最大的 Ca 储存库。Ca 通过内质网中的 SERCA 泵主动泵出,内质网腔中的 Ca 结合蛋白使大量 Ca 得以积累。IP 受体和兰尼碱受体以受控的方式介导 Ca 的释放,从而在细胞内引发复杂的时空信号。内质网中约 500 μM 的 Ca 稳态浓度是由 SERCA 介导的 Ca 摄取和 Ca 被动泄漏之间的平衡产生的。内质网的 Ca 被动泄漏通常被忽略,但根据细胞环境,它可以发挥重要的生理作用。此外,与正常情况相比,过量的 Ca 泄漏会显著降低 ER 中储存的 Ca 量,从而限制了引发 Ca 信号和/或导致 ER 应激的可能性,导致病理后果。然而,尽管已经提出了 20 多种不同的蛋白质可能与之相关,但负责从 ER 漏出 Ca 的所谓“Ca 泄漏通道”仍未得到很好的理解。这篇综述的目的是批判性地评估关于各种潜在相关通道的现有证据,并得出关于它们相对重要性的结论。